Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 14 |
NetGPI | no | yes: 0, no: 14 |
Related structures:
AlphaFold database: A4HEA1
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 15 |
GO:0006793 | phosphorus metabolic process | 3 | 15 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 15 |
GO:0006807 | nitrogen compound metabolic process | 2 | 15 |
GO:0008152 | metabolic process | 1 | 15 |
GO:0009987 | cellular process | 1 | 15 |
GO:0016310 | phosphorylation | 5 | 15 |
GO:0019538 | protein metabolic process | 3 | 15 |
GO:0036211 | protein modification process | 4 | 15 |
GO:0043170 | macromolecule metabolic process | 3 | 15 |
GO:0043412 | macromolecule modification | 4 | 15 |
GO:0044237 | cellular metabolic process | 2 | 15 |
GO:0044238 | primary metabolic process | 2 | 15 |
GO:0071704 | organic substance metabolic process | 2 | 15 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 15 |
GO:0003824 | catalytic activity | 1 | 15 |
GO:0004672 | protein kinase activity | 3 | 15 |
GO:0005488 | binding | 1 | 15 |
GO:0005524 | ATP binding | 5 | 15 |
GO:0016301 | kinase activity | 4 | 15 |
GO:0016740 | transferase activity | 2 | 15 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 15 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 15 |
GO:0017076 | purine nucleotide binding | 4 | 15 |
GO:0030554 | adenyl nucleotide binding | 5 | 15 |
GO:0032553 | ribonucleotide binding | 3 | 15 |
GO:0032555 | purine ribonucleotide binding | 4 | 15 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 15 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 15 |
GO:0036094 | small molecule binding | 2 | 15 |
GO:0043167 | ion binding | 2 | 15 |
GO:0043168 | anion binding | 3 | 15 |
GO:0097159 | organic cyclic compound binding | 2 | 15 |
GO:0097367 | carbohydrate derivative binding | 2 | 15 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 15 |
GO:1901265 | nucleoside phosphate binding | 3 | 15 |
GO:1901363 | heterocyclic compound binding | 2 | 15 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.259 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.333 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.259 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.185 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.463 |
CLV_PCSK_PC1ET2_1 | 99 | 101 | PF00082 | 0.163 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.669 |
DEG_APCC_DBOX_1 | 113 | 121 | PF00400 | 0.283 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.375 |
DEG_SCF_FBW7_1 | 160 | 166 | PF00400 | 0.163 |
DEG_SPOP_SBC_1 | 472 | 476 | PF00917 | 0.445 |
DOC_ANK_TNKS_1 | 75 | 82 | PF00023 | 0.264 |
DOC_CDC14_PxL_1 | 431 | 439 | PF14671 | 0.534 |
DOC_CKS1_1 | 140 | 145 | PF01111 | 0.264 |
DOC_CKS1_1 | 160 | 165 | PF01111 | 0.218 |
DOC_CKS1_1 | 200 | 205 | PF01111 | 0.259 |
DOC_MAPK_gen_1 | 132 | 141 | PF00069 | 0.241 |
DOC_MAPK_gen_1 | 76 | 84 | PF00069 | 0.259 |
DOC_MAPK_MEF2A_6 | 494 | 501 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 76 | 84 | PF00069 | 0.260 |
DOC_PP4_MxPP_1 | 501 | 504 | PF00568 | 0.467 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.163 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.152 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.138 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.671 |
DOC_USP7_UBL2_3 | 276 | 280 | PF12436 | 0.646 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.283 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.264 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.242 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.276 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.241 |
LIG_14-3-3_CanoR_1 | 363 | 370 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 427 | 431 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 486 | 493 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 531 | 540 | PF00244 | 0.551 |
LIG_Actin_WH2_2 | 347 | 365 | PF00022 | 0.300 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.275 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.224 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.515 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.282 |
LIG_FHA_2 | 301 | 307 | PF00498 | 0.259 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.330 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.761 |
LIG_FHA_2 | 555 | 561 | PF00498 | 0.503 |
LIG_LIR_Apic_2 | 202 | 208 | PF02991 | 0.293 |
LIG_LIR_Apic_2 | 268 | 274 | PF02991 | 0.613 |
LIG_LIR_Apic_2 | 35 | 41 | PF02991 | 0.264 |
LIG_LIR_Apic_2 | 467 | 473 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 303 | 313 | PF02991 | 0.259 |
LIG_LIR_Gen_1 | 517 | 527 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 560 | 568 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 429 | 434 | PF02991 | 0.665 |
LIG_LIR_Nem_3 | 517 | 523 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 556 | 561 | PF02991 | 0.534 |
LIG_LYPXL_yS_3 | 445 | 448 | PF13949 | 0.433 |
LIG_MYND_1 | 373 | 377 | PF01753 | 0.264 |
LIG_SH2_CRK | 272 | 276 | PF00017 | 0.591 |
LIG_SH2_CRK | 520 | 524 | PF00017 | 0.425 |
LIG_SH2_GRB2like | 271 | 274 | PF00017 | 0.593 |
LIG_SH2_NCK_1 | 305 | 309 | PF00017 | 0.348 |
LIG_SH2_PTP2 | 157 | 160 | PF00017 | 0.163 |
LIG_SH2_SRC | 157 | 160 | PF00017 | 0.163 |
LIG_SH2_STAP1 | 112 | 116 | PF00017 | 0.259 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.465 |
LIG_SH2_STAP1 | 291 | 295 | PF00017 | 0.289 |
LIG_SH2_STAP1 | 358 | 362 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.163 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.370 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.375 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.259 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.260 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.615 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.737 |
LIG_SUMO_SIM_anti_2 | 560 | 566 | PF11976 | 0.406 |
LIG_TRAF2_1 | 44 | 47 | PF00917 | 0.351 |
LIG_TYR_ITSM | 301 | 308 | PF00017 | 0.318 |
LIG_WW_1 | 263 | 266 | PF00397 | 0.656 |
MOD_CDK_SPK_2 | 181 | 186 | PF00069 | 0.225 |
MOD_CDK_SPxxK_3 | 139 | 146 | PF00069 | 0.375 |
MOD_CDK_SPxxK_3 | 181 | 188 | PF00069 | 0.225 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.496 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.373 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.593 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.712 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.646 |
MOD_CK1_1 | 535 | 541 | PF00069 | 0.651 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.375 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.687 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.259 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.297 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.614 |
MOD_CK2_1 | 506 | 512 | PF00069 | 0.628 |
MOD_CK2_1 | 554 | 560 | PF00069 | 0.505 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.210 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.526 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.323 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.325 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.709 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.698 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.684 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.598 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.636 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.708 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.405 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.207 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.353 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.736 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.254 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.209 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.598 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.687 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.494 |
MOD_N-GLC_1 | 403 | 408 | PF02516 | 0.528 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.375 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.742 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.608 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.368 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.633 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.555 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.674 |
MOD_NEK2_2 | 480 | 485 | PF00069 | 0.506 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.163 |
MOD_PKA_1 | 379 | 385 | PF00069 | 0.575 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.206 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.226 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.322 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.590 |
MOD_PKA_2 | 485 | 491 | PF00069 | 0.701 |
MOD_PKA_2 | 530 | 536 | PF00069 | 0.621 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.290 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.443 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.599 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.375 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.264 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.406 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.242 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.673 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.276 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.698 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.241 |
TRG_DiLeu_BaEn_1 | 560 | 565 | PF01217 | 0.408 |
TRG_DiLeu_BaEn_2 | 346 | 352 | PF01217 | 0.264 |
TRG_DiLeu_BaEn_4 | 46 | 52 | PF01217 | 0.163 |
TRG_DiLeu_BaLyEn_6 | 432 | 437 | PF01217 | 0.535 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.163 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.597 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 558 | 561 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 185 | 188 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 523 | 526 | PF00400 | 0.544 |
TRG_NES_CRM1_1 | 118 | 133 | PF08389 | 0.375 |
TRG_NLS_MonoExtN_4 | 277 | 284 | PF00514 | 0.458 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8W2 | Leptomonas seymouri | 55% | 95% |
A0A0N1HZY0 | Leptomonas seymouri | 27% | 95% |
A0A0S4JPZ7 | Bodo saltans | 26% | 100% |
A0A1X0NYS1 | Trypanosomatidae | 42% | 100% |
A0A3S7WY10 | Leishmania donovani | 26% | 100% |
A0A3S7WZA6 | Leishmania donovani | 78% | 99% |
A0A422P4L8 | Trypanosoma rangeli | 45% | 100% |
A4H459 | Leishmania braziliensis | 25% | 100% |
A4HD79 | Leishmania braziliensis | 26% | 100% |
A4HFC9 | Leishmania braziliensis | 24% | 86% |
A4I1P7 | Leishmania infantum | 77% | 98% |
C9ZK98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AWL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AXT1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 99% |
Q1PFB9 | Arabidopsis thaliana | 25% | 100% |
Q4Q9P0 | Leishmania major | 77% | 100% |
Q4QH29 | Leishmania major | 24% | 100% |
Q54JG7 | Dictyostelium discoideum | 24% | 100% |
Q99078 | Ustilago maydis (strain 521 / FGSC 9021) | 25% | 100% |